Charadriiformes









































Charadriiformes
Temporal range: Late Cretaceous-Present, 75–0 Ma

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חופמאים-01.jpg
Several members of the order

Scientific classification edit
Kingdom:
Animalia
Phylum:
Chordata
Class:
Aves
Infraclass:
Neognathae

Clade:

Neoaves

Clade:

Aequorlitornithes
Order:
Charadriiformes
Huxley, 1867
Families

See text.



Charadriiformes is a diverse order of small to medium-large birds. It includes about 350 species and has members in all parts of the world. Most Charadriiformes live near water and eat invertebrates or other small animals; however, some are pelagic (seabirds), some occupy deserts and a few are found in thick forest.




Contents






  • 1 Taxonomy, systematics and evolution


    • 1.1 Families in taxonomic order


    • 1.2 Evolution history




  • 2 Evolution of parental care in Charadriiformes


  • 3 See also


  • 4 Footnotes


  • 5 References





Taxonomy, systematics and evolution


The order was formerly divided into three suborders:



  • The waders (or "Charadrii"): typical shorebirds, most of which feed by probing in the mud or picking items off the surface in both coastal and freshwater environments.

  • The gulls and their allies (or "Lari"): these are generally larger species which take fish from the sea. Several gulls and skuas will also take food items from beaches, or rob smaller species, and some have become adapted to inland environments.

  • The auks (or "Alcae") are coastal species which nest on sea cliffs and "fly" underwater to catch fish.


The Sibley-Ahlquist taxonomy, which has been widely accepted in America,[citation needed] lumps all the Charadriiformes together with other seabirds and birds of prey into a greatly enlarged order Ciconiiformes. However, the resolution of the DNA-DNA hybridization technique used by Sibley & Ahlquist was not sufficient to properly resolve the relationships in this group, and indeed it appears as if the Charadriiformes constitute a single large and very distinctive lineage of modern birds of their own.[1]


The auks, usually considered distinct because of their peculiar morphology, are more likely related to gulls, the "distinctness" being a result of adaptation for diving. Following recent research,[2] a better arrangement may be as follows:



Families in taxonomic order


This is a list of the charadriiform families, presented in taxonomic order.




  • Suborder Scolopaci: snipe-like waders
    • Family Scolopacidae: snipe, sandpipers, phalaropes, and allies



  • Suborder Thinocori: aberrant charadriforms

    • Family Rostratulidae: painted snipe

    • Family Jacanidae: jacanas

    • Family Thinocoridae: seedsnipe

    • Family Pedionomidae: plains wanderer




  • Suborder Lari: gulls and allies

    • Family Laridae: gulls, terns, and skimmers

    • Family Alcidae: puffins, guillemots, murres, and allies

    • Family Stercorariidae: skuas

    • Family Glareolidae: pratincoles and coursers

    • Family Pluvianidae: Egyptian plover

    • Family Dromadidae: crab plover




  • Suborder Turnici: buttonquails
    • Family Turnicidae: buttonquails



  • Suborder Chionidi: thick-knees and allies

    • Family Burhinidae: thick-knees

    • Family Chionididae: sheathbills

    • Family Pluvianellidae: Magellanic plover




  • Suborder Charadrii: plover-like waders

    • Family Ibidorhynchidae: ibisbill

    • Family Recurvirostridae: avocets and stilts

    • Family Haematopodidae: oystercatchers

    • Family Charadriidae: plovers and lapwings




More conservatively, the Thinocori could be included in the Scolopaci (this combined sub-order is called Limicoli), and the Chionidi in the Charadrii. The suborders Thincori, Scolopaci, Chionidi, and Charadri are commonly referred to collectively as waders. Some taxonomy sources place the family Glareolidae in its own suborder, instead of being classified under suborder Lari.[3] The buttonquails are of indeterminate or basal position in the Lari-Scolopaci sensu lato group. The arrangement as presented here is a consensus of the recent studies.[4]


.mw-parser-output table.clade{border-spacing:0;margin:0;font-size:100%;line-height:100%;border-collapse:separate;width:auto}.mw-parser-output table.clade table.clade{width:100%}.mw-parser-output table.clade td{border:0;padding:0;vertical-align:middle;text-align:center}.mw-parser-output table.clade td.clade-label{width:0.8em;border:0;padding:0 0.2em;vertical-align:bottom;text-align:center}.mw-parser-output table.clade td.clade-slabel{border:0;padding:0 0.2em;vertical-align:top;text-align:center}.mw-parser-output table.clade td.clade-bar{vertical-align:middle;text-align:left;padding:0 0.5em}.mw-parser-output table.clade td.clade-leaf{border:0;padding:0;text-align:left;vertical-align:middle}.mw-parser-output table.clade td.clade-leafR{border:0;padding:0;text-align:right}






Charadriiformes














Charadrii














Chionida














Burhinidae













 

Burhinus


 
 

Esacus


 

 
 














Chionidae

Chionis


 

Pluvianellidae

Pluvianellus


 

 

 

Charadriida














Pluvianidae

Pluvianus


 
 













 














Pluvialidae

Pluvialis


 
 













 














Ibidorhynchidae

Ibidorhyncha


 

Haematopodidae

Haematopus


 

 

Recurvirostridae













 

Recurvirostra


 
 













 

Cladorhynchus


 
 

Himantopus


 

 

 

 

 

Charadriidae














Charadriinae













 

Oreopholus


 
 













 













 

Phegornis


 
 

Zonibyx


 

 
 













 

Eudromias


 
 













 

Afroxyechus


 
 













 

Charadrius


 
 

Thinornis


 

 

 

 

 

 
 














Vanellinae

Vanellus


 

Anarhynchinae













 

Erythrogonys


 
 













 

Peltohyas


 
 













 

Eupoda


 
 













 

Anarhynchus


 
 

Ochthodromus


 

 

 

 

 

 

 

 

 

 
 














Limicoli














Jacanida













Thincoroidea














Pedionomidae

Pedionomus


 

Thinocoridae













 

Attagis


 
 

Thinocorus


 

 

 
Jacanoidea














Rostratulidae













 

Nycticryphes


 
 

Rostratula


 

 

Jacanidae













 













 

Hydrophasianus


 
 

Jacana


 

 
 













 

Actophilornis


 
 













 

Metopidius


 
 













 

Microparra


 
 

Irediparra


 

 

 

 

 

 

 

Scolopacida









Scolopacidae














Numeniinae













 

Bartramia


 
 

Numenius


 

 
 














Limosinae

Limosa


 
 














Arenariinae























 

Limicola


 
 

Ereunetes


 
 

Calidris


 
 













 

Arenaria


 
 

Prosobonia


 

 

 
 














Tringinae













 













 

Xenus


 
 

Phalaropus


 

 
 













 

Actitis


 
 

Tringa


 

 

 

Scolopacinae













 













 

Lymnocryptes


 
 

Limnodromus


 

 
 













 

Scolopax


 
 













 

Gallinago


 
 













 

Chubbia


 
 

Coenocorypha


 

 

 

 

 

 

 

 

 

 

 

Lari














Turnicida













 

Ortyxelos


 
 

Turnix


 

 

Larida













Glareoloidea














Dromadidae

Dromas ardeola


 

Glareolidae


















 

Stiltia


 
 

Rhinoptilus


 
 













 

Cursorius


 
 

Glareola


 

 

 

 
 













Alcoidea














Stercorariidae

Stercorarius


 

Alcidae














Fraterculinae













 













 

Cerorhinca


 
 

Fratercula


 

 
 













 

Ptychoramphus


 
 

Aethia


 

 

 

Alcinae













 

Brachyramphus


 
 













 

Cepphus


 
 













 

Synthliboramphus


 
 













 













 

Uria


 
 

Alle


 

 
 













 

Alca


 
 

†Pinguinus


 

 

 

 

 

 

 

 
Laroidea









Laridae





























Gyginae

Gygis


 

Rynchopinae

Rynchops


 

Anoinae













 

Anous


 
 

Procelsterna


 

 

Sterninae













 

Onychoprion


 
 













 

Sternula


 
 













 

Phaetusa


 
 













 













 

Gelochelidon


 
 

Hydroprogne


 

 
 













 

Larosterna


 
 













 

Chlidonias


 
 













 

Thalasseus


 
 

Sterna


 

 

 

 

 

 

 

 

Larinae























 

Creagrus


 
 













 

Hydrocoloeus


 
 

Rhodostethia


 

 
 













 

Rissa


 
 













 

Pagophila


 
 

Xema


 

 

 
 













 

Saundersilarus


 
 













 

Chroicocephalus


 
 













 

Leucophaeus


 
 













 

Larus


 
 

Ichthyaetus


 

 

 

 

 

 

 

 

 

 

 

 

 

Cladogram based on Baker, A.J. et al. (2012)[5] and Boyd, J. H. et al. (2016) [3]



Evolution history


That the Charadriiformes are an ancient group is also borne out by the fossil record. Much of the Neornithes' fossil record around the Cretaceous–Paleogene extinction event is made up of bits and pieces of birds which resemble this order. In many, this is probably due to convergent evolution brought about by semiaquatic habits. Specimen VI 9901 (López de Bertodano Formation, Late Cretaceous of Vega Island, Antarctica) is probably a basal charadriiform somewhat reminiscent of a thick-knee.[6] However, more complete remains of undisputed charadriiforms are known only from the mid-Paleogene onwards. Present-day orders emerged around the Eocene-Oligocene boundary, roughly 35-30 mya. Basal or unresolved charadriiforms are:




  • "Morsoravis" (Late Paleocene/Early Eocene of Jutland, Denmark) - a nomen nudum?


  • Jiliniornis (Huadian Middle Eocene of Huadian, China) - charadriid?


  • Boutersemia (Early Oligocene of Boutersem, Belgium) - glareolid?


  • Turnipax (Early Oligocene) - turnicid?


  • Elorius (Early Miocene Saint-Gérand-le-Puy, France)


  • "Larus" desnoyersii (Early Miocene of SE France) - larid? stercorarid?


  • "Larus" pristinus (John Day Early Miocene of Willow Creek, USA) - larid?

  • Charadriiformes gen. et sp. indet. (Bathans Early/Middle Miocene of Otago, New Zealand) - charadriid? scolopacid?[7]

  • Charadriiformes gen. et sp. indet. (Bathans Early/Middle Miocene of Otago, New Zealand) - charadriid? scolopacid?[8]

  • Charadriiformes gen. et sp. indet. (Bathans Early/Middle Miocene of Otago, New Zealand) - larid?[9]

  • Charadriiformes gen. et sp. indet. (Sajóvölgyi Middle Miocene of Mátraszõlõs, Hungary[10]


  • "Totanus" teruelensis (Late Miocene of Los Mansuetos, Spain) - scolopacid? larid?


The "transitional shorebirds" ("Graculavidae") are a generally Mesozoic form taxon formerly believed to constitute the common ancestors of charadriiforms, waterfowl and flamingos. They are now assumed to be mostly basal taxa of the charadriiforms and/or "higher waterbirds", which probably were two distinct lineages 65 mya already,[citation needed] and few if any are still believed to be related to the well-distinct waterfowl. Taxa formerly considered graculavids are:




  • Laornithidae - charadriiform? gruiform?

    • Laornis (Late Cretaceous?)



  • "Graculavidae"


    • Graculavus (Lance Creek Late Cretaceous - Hornerstown Late Cretaceous/Early Palaeocene) - charadriiform?


    • Palaeotringa (Hornerstown Late Cretaceous?) - charadriiform?


    • Telmatornis (Navesink Late Cretaceous?) - charadriiform? gruiform?


    • Scaniornis - phoenicopteriform?


    • Zhylgaia - presbyornithid?

    • Dakotornis

    • "Graculavidae" gen. et sp. indet. (Gloucester County, USA)




Other wader- or gull-like birds incertae sedis, which may or may not be Charadriiformes, are:




  • Ceramornis (Lance Creek Late Cretaceous)


  • "Cimolopteryx" (Lance Creek Late Cretaceous)


  • Palintropus (Lance Creek Late Cretaceous)


  • Torotix (Late Cretaceous)


  • Volgavis (Early Paleocene of Volgograd, Russia)


  • Eupterornis (Paleocene of France)

  • Neornithes incerta sedis (Late Paleocene/Early Eocene of Ouled Abdoun Basin, Morocco)[11]


  • Fluviatitavis (Early Eocene of Silveirinha, Portugal)



Evolution of parental care in Charadriiformes


Shorebirds pursue a larger diversity of parental care strategies than do most other avian orders. They therefore present an attractive set of examples to support the understanding of the evolution of parental care in avians generally (as reviewed in Thomas et al. 2007). The ancestral avian most likely had a female parental care system (Tullberg et al. 2002). The shorebird ancestor specifically evolved from a bi-parental care system, yet the species within the clade Scolopacidae evolved from a male parental care system. These transitions might have occurred for several reasons. Brooding density is correlated with male parental care. Male care systems in birds are shown to have a very low breeding density while female care systems in birds have a high breeding density. (Owens 2005). Certain rates of male and female mortality, male and female egg maturation rate, and egg death rate have been associated with particular systems as well (Klug et al. 2013). It has also been shown that sex role reversal is motivated by the male-biased adult sex ratio (Liker et al. 2013). The reason for such diversity in shorebirds, compared to other birds, has yet to be understood.



See also


  • List of Charadriiformes by population


Footnotes





  1. ^ Fain & Houde (2004)


  2. ^ Ericson et al. (2003), Paton et al. (2003), Thomas et al. (2004a,b), van Tuinen et al. (2004), Paton & Baker (2006)


  3. ^ ab John, Boyd. "Charadriiformes". jboyd.net. Retrieved 2017-07-16..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}


  4. ^ van Tuinen et al. (2004), Paton & Baker (2006)


  5. ^ Baker, A.J. et al. (2012) Eight independent nuclear genes support monophyly of the plovers: The role of mutational variance in gene trees.


  6. ^ Case, J. A. and C. P. Tambussi. 1999. Maastrichtian record of neornithine birds in Antarctica: comments on a Late Cretaceous radiation


  7. ^ Proximal right humerus (MNZ S42416) and proximal left carpometacarpi (MNZ S42415, S42435) of a bird the size of a red-necked stint: Worthy et al. (2007)


  8. ^ Several wing and thorax bones of a bird the size of a double-banded plover: Worthy et al. (2007)


  9. ^ Premaxillae (MNZ S42681, S42736) and proximal right scapula (MNZ S41058) of a bird apparently similar to the black-billed gull but almost the size of a kelp gull: Worthy et al. (2007)


  10. ^ Gál et al. (1998-99)


  11. ^ A wading bird the size of a white stork (Ciconia ciconia): Bourdon (2005)




References



  • Bourdon, Estelle (2006): L'avifaune du Paléogène des phosphates du Maroc et du Togo: diversité, systématique et apports à la connaissance de la diversification des oiseaux modernes (Neornithes) ["Paleogene avifauna of phosphates of Morocco and Togo: diversity, systematics and contributions to the knowledge of the diversification of the Neornithes"]. Doctoral thesis, Muséum national d'histoire naturelle [in French]. HTML abstract

  • Ericson, Per G.P.; Envall, I.; Irestedt, M. & Norman, J.A. (2003): Inter-familial relationships of the shorebirds (Aves: Charadriiformes) based on nuclear DNA sequence data. BMC Evol. Biol. 3: 16. doi:10.1186/1471-2148-3-16 PDF fulltext

  • Fain, Matthew G. & Houde, Peter (2004): Parallel radiations in the primary clades of birds. Evolution 58(11): 2558-2573. doi:10.1554/04-235
    PMID 15612298
    PDF fulltext

  • Gál, Erika; Hír, János; Kessler, Eugén & Kókay, József (1998–99): Középsõ-miocén õsmaradványok, a Mátraszõlõs, Rákóczi-kápolna alatti útbevágásból. I. A Mátraszõlõs 1. lelõhely [Middle Miocene fossils from the sections at the Rákóczi chapel at Mátraszőlős. Locality Mátraszõlõs I.]. Folia Historico Naturalia Musei Matraensis 23: 33-78. [Hungarian with English abstract] PDF fulltext

  • Klug, H., M. B. Bonsall, and S.H Alonzo. 2013. Sex differences in life history drive evolutionary transitions among maternal, paternal, and bi‐parental care. Ecology and Evolution. 3: 792–806.

  • Liker, A., R. P. Freckleton, and T. Székely. 2013. The evolution of sex roles in birds is related to adult sex ratio. Nature Communications. 4: 1587.

  • Owens, I.P. 2002. Male–only care and classical polyandry in birds: phylogeny, ecology and sex differences in remating opportunities. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 357: 283-293.

  • Paton, Tara A. & Baker, Allan J. (2006): Sequences from 14 mitochondrial genes provide a well-supported phylogeny of the Charadriiform birds congruent with the nuclear RAG-1 tree. Mol. Phylogenet. Evol. 39(3): 657–667. doi:10.1016/j.ympev.2006.01.011
    PMID 16531074
    (HTML abstract)

  • Paton, T.A.; Baker, A.J.; Groth, J.G. & Barrowclough, G.F. (2003): RAG-1 sequences resolve phylogenetic relationships within charadriiform birds. Mol. Phylogenet. Evol. 29: 268-278. doi:10.1016/S1055-7903(03)00098-8
    PMID 13678682
    (HTML abstract)

  • Székely, T and J.D. Reynolds. 1995. Evolutionary transitions in parental care in shorebirds. Proceedings of the Royal Society of London. Series B: Biological Sciences. 262: 57-64.

  • Thomas, G. H., T. Székely and J.D. Reynolds. 2007. Sexual conflict and the evolution of breeding systems in shorebirds. Advances in the Study of Behavior. 37: 279-342.

  • Thomas, Gavin H.; Wills, Matthew A. & Székely, Tamás (2004a): Phylogeny of shorebirds, gulls, and alcids (Aves: Charadrii) from the cytochrome-b gene: parsimony, Bayesian inference, minimum evolution, and quartet puzzling. Mol. Phylogenet. Evol. 30(3): 516-526. doi:10.1016/S1055-7903(03)00222-7 (HTML abstract)

  • Thomas, Gavin H.; Wills, Matthew A. & Székely, Tamás (2004): A supertree approach to shorebird phylogeny. BMC Evol. Biol. 4: 28. doi:10.1186/1471-2148-4-28
    PMID 15329156
    [1]Template:Date=November 2018 Supplementary Material[permanent dead link]

  • Tullberg, B. S., M. Ah–King and H. Temrin. 2002. Phylogenetic reconstruction of parental–care systems in the ancestors of birds. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 357: 251-257.

  • van Tuinen, Marcel; Waterhouse, David & Dyke, Gareth J. (2004): Avian molecular systematics on the rebound: a fresh look at modern shorebird phylogenetic relationships. J. Avian Biol. 35(3): 191-194. doi:10.1111/j.0908-8857.2004.03362.x PDF fulltext


  • Worthy, Trevor H.; Tennyson, A.J.D.; Jones, C.; McNamara, J.A. & Douglas, B.J. (2007): Miocene waterfowl and other birds from central Otago, New Zealand. J. Syst. Palaeontol. 5(1): 1-39. doi:10.1017/S1477201906001957 (HTML abstract)











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